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Clinical Trial Summary

This is a monocenter, open-label, uncontrolled study in accordance with §23b MPG to evaluate the efficacy of the HIFU-treatment of fibroadenoma using the TH-One device

Objectives Primary objective: To evaluate the efficacy of HIFU in the treatment of the breast fibroadenoma using the TH-One device Secondary objective: To evaluate the tolerability of the HIFU using the TH-One device


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02011919
Study type Interventional
Source Theraclion
Contact
Status Completed
Phase N/A
Start date December 2013
Completion date January 2017

See also
  Status Clinical Trial Phase
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Active, not recruiting NCT01331954 - Treatment of Breast Fibroadenoma With High Intensity Focused Ultrasound (HIFU) N/A
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Recruiting NCT03044054 - Treatment of Breast Fibroadenoma Targeted Tissue With HIFU N/A
Completed NCT02139683 - Feasibility Study Assessing the Treatment of Fibroadenomata With a Circumferential Sonication Treatment With HIFU N/A
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Completed NCT02078011 - Treatment of Breast Fibroadenoma With High Intensity Focused Ultrasound N/A